S100a8 (GeneID: 20201) | Mus musculus
Description: S100 calcium binding protein A8 (calgranulin A) [Source:MGI Symbol;Acc:MGI:88244]
Synonyms: p8, Caga, 60B8Ag, CP-10, B8Ag, RP8, CFAg, AI323541
Other ID(s): ENSMUSG00000056054, MGI:88244
Protein Accession Numbers: NP_038678
Statistics: PTM(8)
Post translational modifications (PTM) by Type

∙ Please click the name of species for the protein accession number used in the alignment.
∙ A p letter used as a pointer to positions of post translational modifications in human.
∙ Protein domains illustrated above belong to Homo sapiens (Human).
∙ ClinVar stacked bar chart represents whole protein isoforms of the gene. Please, check the other protein isoforms of the gene below.
∙ If more than one transcripts below are active (with blue background color), it means all the active transcripts have the same sequence.
ENST00000368732 ENST00000368733 NP_001306125 NP_001306126 You are here now! NP_001306127 NP_001306130 NP_002955


import_contactsClinVar Data
Variation ID filter_list Allele ID filter_list RS Number filter_list Variant Type filter_list Record filter_list Alteration filter_list Clinicial Sig. filter_list Last Update filter_list Phenotypes filter_list Cytogenetic filter_list Review Status filter_list RCV Acc.N. filter_list

healinggnomAD
Variant ID filter_list Transcript ID filter_list Alteration filter_list Annotation filter_list Allele C. filter_list Allele N. filter_list Allele F. filter_list rsNumber filter_list Flagsfilter_list Filter filter_list

placePost-translational Modifications (PTMs)
Gene Name filter_list ACC ID filter_list PTM Type filter_list Position filter_list Mod-rsd filter_list Site +/-7 Aa filter_list Mw_kd filter_list Site grpID filter_list

blur_onCatalogue of Somatic Mutations in Cancer (COSMIC)
Gene Name filter_list Transcript ID filter_list Sample name filter_list Primary Site filter_list Primary Histology filter_list Mutation ID filter_list Mutation CDS filter_list Mutation Aa filter_list Mutation Desc. filter_list FATHMM Prediction filter_list FATHMM Score filter_list Mutation Somatic Status filter_list PUBMED PMID filter_list Tumor Origin filter_list Position filter_list

chrome_reader_modedbSNP
Gene ID filter_list Transcript ID filter_list Consequence filter_list Position filter_list HGVSp filter_list Impact filter_list

format_align_centerProtein Domains (PFAM)
Pfam Domain filter_list Domain Name filter_list Description filter_list Positions filter_list Clan filter_list Clan Name filter_list Organism filter_list
NO RESULT FOUND
PF01023 S_100 S-100/ICaBP type calcium binding domain 5-49 CL0220 EF_hand Homo sapiens

view_listList of the diseases from DisGeNET
Disease Name filter_list Disease Category filter_list DSI* filter_list DPI** filter_list
Dermatitis, Atopic Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Skin and Connective Tissue Diseases ; Immune System Diseases ; 0.481 0.828
Contact Dermatitis Skin and Connective Tissue Diseases ; 0.481 0.828
Keloid Skin and Connective Tissue Diseases ; Pathological Conditions, Signs and Symptoms ; 0.481 0.828
Leukemia, Myelocytic, Acute Neoplasms ; 0.481 0.828
Animal Mammary Neoplasms Neoplasms ; Animal Diseases ; 0.481 0.828
Acute Myeloid Leukemia, M1 Neoplasms ; 0.481 0.828
Eczema, Infantile Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Skin and Connective Tissue Diseases ; Immune System Diseases ; 0.481 0.828
Contact hypersensitivity Skin and Connective Tissue Diseases ; 0.481 0.828
Mammary Carcinoma, Animal Neoplasms ; Animal Diseases ; 0.481 0.828
Acute Myeloid Leukemia (AML-M2) Neoplasms ; 0.481 0.828
NO RESULT FOUND
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